CLA-1/SR-BI is expressed in atherosclerotic lesion macrophages and regulated by activators of peroxisome proliferator-activated receptors

Circulation. 2000 May 23;101(20):2411-7. doi: 10.1161/01.cir.101.20.2411.

Abstract

Background: The scavenger receptors are cell-surface receptors for native and modified lipoproteins that play a critical role in the accumulation of lipids by macrophages. CLA-1/SR-BI binds HDL with high affinity and is involved in the cholesterol reverse-transport pathway. Peroxisome proliferator-activated receptors (PPARs) are transcription factors regulating the expression of genes implicated in lipid metabolism, cellular differentiation, and inflammation. Here, we investigated the expression of CLA-1/SR-BI in macrophages and its regulation by PPARs.

Methods and results: CLA-1 is undetectable in human monocytes and is induced upon differentiation into macrophages. Immunohistological analysis on human atherosclerotic lesions showed high expression of CLA-1 in macrophages of the lipid core colocalizing with PPARalpha and PPARgamma staining. Activation of PPARalpha and PPARgamma resulted in the induction of CLA-1 protein expression in monocytes and in differentiated macrophages. Finally, SR-BI expression is increased in atherosclerotic lesions of apoE-null mice treated with either PPARgamma or PPARalpha ligands.

Conclusions: Our data demonstrate that CLA-1/SR-BI is expressed in atherosclerotic lesion macrophages and induced by PPAR activation, identifying a potential role for PPARs in cholesterol homeostasis in atherosclerotic lesion macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apolipoproteins E / deficiency
  • Arteriosclerosis / metabolism*
  • Arteriosclerosis / pathology
  • CD36 Antigens / metabolism*
  • Cell Differentiation
  • Cells, Cultured
  • Female
  • Humans
  • Ligands
  • Macrophages / cytology
  • Macrophages / metabolism*
  • Membrane Proteins*
  • Mice
  • Mice, Inbred C57BL
  • Monocytes / cytology
  • Monocytes / metabolism
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Receptors, Immunologic*
  • Receptors, Lipoprotein*
  • Receptors, Scavenger
  • Scavenger Receptors, Class B
  • Stimulation, Chemical
  • Transcription Factors / physiology*

Substances

  • Apolipoproteins E
  • CD36 Antigens
  • Ligands
  • Membrane Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Immunologic
  • Receptors, Lipoprotein
  • Receptors, Scavenger
  • SCARB1 protein, human
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • Transcription Factors